Variant report

Variant	rs16845010
Chromosome Location	chr3:102116258-102116259
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12107279	1.00[AMR][1000 genomes]
rs1399767	1.00[AMR][1000 genomes]
rs1399768	1.00[AMR][1000 genomes]
rs16844987	1.00[AMR][1000 genomes]
rs16844991	1.00[AMR][1000 genomes]
rs16845005	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16845028	1.00[AMR][1000 genomes]
rs16845031	1.00[AMR][1000 genomes]
rs16845051	1.00[AMR][1000 genomes]
rs16845092	1.00[AMR][1000 genomes]
rs16845152	1.00[AMR][1000 genomes]
rs16845154	1.00[AMR][1000 genomes]
rs16845157	1.00[AMR][1000 genomes]
rs57555073	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877227	chr3:102067254-102184308	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv1007340	chr3:102108954-102725099	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv536676	chr3:102108954-102725099	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:102111400-102117200	Weak transcription	Fetal Brain Male	brain
2	chr3:102113800-102117200	Weak transcription	NHEK	skin
3	chr3:102113800-102118600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr3:102114000-102118000	Weak transcription	HMEC	breast
5	chr3:102114000-102119000	Weak transcription	HSMM	muscle
6	chr3:102114200-102117600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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